Package 42708-110-60
Brand: metoprolol tartrate
Generic: metoprolol tartratePackage Facts
Identity
Package NDC
42708-110-60
Digits Only
4270811060
Product NDC
42708-110
Description
60 TABLET, FILM COATED in 1 BOTTLE (42708-110-60)
Marketing
Marketing Status
Brand
metoprolol tartrate
Generic
metoprolol tartrate
Sample Package
Yes
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459c810c-930f-6de5-e063-6394a90a48db", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["85a638c3-d53c-453d-935c-fcfd31372a45"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "60 TABLET, FILM COATED in 1 BOTTLE (42708-110-60)", "package_ndc": "42708-110-60", "marketing_start_date": "20180426"}], "brand_name": "Metoprolol Tartrate", "product_id": "42708-110_459c810c-930f-6de5-e063-6394a90a48db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42708-110", "generic_name": "Metoprolol Tartrate", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20261231"}